Kristiana Page,  —

Kristiana Page is a passionate writer, jiujiteira, and lover of crunchy salt and vinegar chips. She lives in Geelong, Victoria, Australia. She was diagnosed with stage V lupus nephritis in 2016 at the age of 20. True to her personality, her writing is emotional, honest — sometimes blunt — and largely undeterred by what other people might think. For her, writing is equal parts therapy and the ultimate act of defiance against an invisible illness that thrived off her silence. She loves to use words to reduce stigma, shine a light on the realities of life with an invisible illness, and make the world feel a little smaller when it matters most.

Articles by Kristiana Page

What a Photo Can’t Tell You

Can you guess which one of us is sick? If I were to show you this picture (on the left) and ask you to pick out which one of us is sick, which one of us would you choose? Would you take a wild guess,…

Acknowledge, Embrace the Strength That Comes in Numbers

Since I began writing this column, I’ve had many people reach out to me. Sometimes it’s because an article deeply resonated or helped them express something for the first time. Occasionally readers will deliver a virtual hug because what I’ve described is too familiar and hits close to…

More Than Just a Number

Medicine can’t tell you much about lupus, but it loves to throw out facts. If you Google lupus right now, a range of statistics will pop up. According to Monash University, lupus affects 5 million people worldwide. It’s most predominate in the 15-44 year old age…

Dear Potential Partner, Thanks for Understanding

We haven’t been seeing each other very long, and honestly I’m still undecided as to whether you’re “Mr. Right,” “Mr. Right Now,” or something between. But regardless of the context we’re in, the prospect of this new relationship simultaneously excites me and scares me; while there’s so…

The Ebb and Flow of Lupus Fatigue

More and more I’m learning that with lupus, nothing has any kind of permanency. I have days free of fatigue, and I feel so good that I question whether I’m really chronically ill. But those days never last. Not long after, I find myself hit with another…

Finding Strength to Fight Lupus Creates Barriers to Love

Lupus was the ultimate wrench in the works. There isn’t one aspect of my life that went untouched; nothing was safe or left unchanged. I have to admit that in most cases it’s been a positive thing. However, when it comes to love, I can’t bring myself…

The Incredible Irony of My Life with Lupus

There was a period of time, not long after my diagnosis, when I felt as if I had truly lost everything. I felt overcome by my condition, as if it had sucked all the goodness out of every aspect of my life. Today, I find myself on…

Living with Lupus and The ‘Little Wins’

When it came to my first six months with lupus, it felt like I took so many losses. My diet, my energy, my face, my body shape, the list just kept growing. I felt like I never got to take anything back. I never got to have a…

A Tribute to Strong Women

I write this in a state of disbelief and heartbroken shock. Not long ago I found out about the passing of someone whose presence merely graced my life, yet left a lasting imprint. I’d love to dedicate this column not only to one wonderful and strong woman,…